← Back to catalogue

Instant Cold Pack

EUDAMED

Class IIa (EU MDR)

Ref KK-IC-B 230

by Koolcare Technology Co., Ltd.

Identity

Device Name
Instant Cold Pack EUDAMED
Model / Reference
KK-IC-B 230 EUDAMED

Identifiers

Primary DI / UDI-DI
06974423592302 EUDAMED
Basic UDI-DI
697442359ICBS3 EUDAMED
EMDN Code
M030504 IMMOBILISATION SYSTEMS, MOULDABLE UNDER COLD AND HOT TEMPERATURES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Instant Cold Pack by Koolcare Technology Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000017687
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED caac9bdf-95f6-4627-b62b-146020c1bbe2 61 fields · synced Jun 19, 2026